Canonical Allele Identifier: CA2333793008

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729841_35729846delinsGGCTGC , CM000681.2:g.35729841_35729846delinsGGCTGC	GRCh38
NC_000019.9:g.36220742_36220747delinsGGCTGC , CM000681.1:g.36220742_36220747delinsGGCTGC	GRCh37
NC_000019.8:g.40912582_40912587delinsGGCTGC	NCBI36
NG_052906.1:g.16823_16828delinsGGCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4852-126_4852-121delinsGGCTGC	ENSP00000501283.1:n.4852-126_4852-121delinsGGCTGC
ENST00000674114.2:c.2459-126_2459-121delinsGGCTGC	ENSP00000501039.2:n.2459-126_2459-121delinsGGCTGC
ENST00000684977.1:c.136-126_136-121delinsGGCTGC	ENSP00000509384.1:n.136-126_136-121delinsGGCTGC
ENST00000685168.1:c.344-126_344-121delinsGGCTGC
ENST00000689544.1:n.71-126_71-121delinsGGCTGC
ENST00000691421.1:c.139-126_139-121delinsGGCTGC	ENSP00000508674.1:n.139-126_139-121delinsGGCTGC
ENST00000691855.1:c.4460-126_4460-121delinsGGCTGC
ENST00000692961.1:c.4918-126_4918-121delinsGGCTGC	ENSP00000509289.1:n.4918-126_4918-121delinsGGCTGC
ENST00000420124.4:c.4918-126_4918-121delinsGGCTGC MANE Select	ENSP00000398837.2:n.4918-126_4918-121delinsGGCTGC
ENST00000673918.1:c.4852-126_4852-121delinsGGCTGC	ENSP00000501283.1:n.4852-126_4852-121delinsGGCTGC
ENST00000674114.1:c.2240-126_2240-121delinsGGCTGC
ENST00000420124.2:c.4918-126_4918-121delinsGGCTGC	ENSP00000398837.1:n.4918-126_4918-121delinsGGCTGC
NM_014727.2:c.4918-126_4918-121delinsGGCTGC	NP_055542.1:n.4918-126_4918-121delinsGGCTGC
XM_011527561.1:c.4852-126_4852-121delinsGGCTGC	XP_011525863.1:n.4852-126_4852-121delinsGGCTGC
XM_011527562.1:c.4918-126_4918-121delinsGGCTGC	XP_011525864.1:n.4918-126_4918-121delinsGGCTGC
XM_011527563.1:c.4642-126_4642-121delinsGGCTGC	XP_011525865.1:n.4642-126_4642-121delinsGGCTGC
XM_011527561.2:c.4354-126_4354-121delinsGGCTGC	XP_011525863.2:n.4354-126_4354-121delinsGGCTGC
XM_011527562.2:c.4918-126_4918-121delinsGGCTGC	XP_011525864.1:n.4918-126_4918-121delinsGGCTGC
XM_017027544.1:c.4918-126_4918-121delinsGGCTGC	XP_016883033.1:n.4918-126_4918-121delinsGGCTGC
XM_017027545.1:c.4354-126_4354-121delinsGGCTGC	XP_016883034.1:n.4354-126_4354-121delinsGGCTGC
XM_017027546.1:c.1882-126_1882-121delinsGGCTGC	XP_016883035.1:n.1882-126_1882-121delinsGGCTGC
NM_014727.3:c.4918-126_4918-121delinsGGCTGC MANE Select	NP_055542.1:n.4918-126_4918-121delinsGGCTGC